Fernando Vallejos-Burgos

Distorted Graphene Sheet Structure-Derived Latent Nanoporosity

High surface area graphene monoliths consist mainly of single graphene layers wider than 10 nm. The interlayer porosity of high temperature treated nanoporous graphene monoliths with tuned intergraphene layer structures is evaluated by hybrid analysis of Ar adsorption at 87 K, N2 adsorption at 77 K, high resolution transmission electron microscopic observation, and small-angle X-ray scattering (SAXS) measurements. SAXS analysis results in surface areas that are 1.4 and 4.5 times larger than those evaluated by Ar adsorption for graphene monoliths nontreated and treated at 2273 K, respectively. A distorted graphene sheet structure model is proposed for the high surface area graphene monoliths on the basis of the hybrid analysis.

Water adsorption property of hierarchically nanoporous detonation nanodiamonds

The detonation nanodiamonds form the aggregate having interparticle voids, giving a marked hygroscopic property. As the relationship between pore structure and water adsorption of aggregated nanodiamonds is not well understood yet, adsorption isotherms of N2 at 77 K and of water vapor at 298 K of the well-characterized aggregated nanodiamonds were measured. HR-TEM and X-ray diffraction showed that the nanodiamonds were highly crystalline and their average crystallite size was 4.5 nm. The presence of the graphitic layers on the nanodiamond particle surface was confirmed by the EELS examination. The pore size distribution analysis showed that nanodiamonds had a few ultramicropores with predominant mesopores of 4.5 nm in average size. The water vapor adsorption isotherm of IUPAC Type V indicates the hydrophobicity of the nanodiamond aggregates, with the presence of hydrophilic sites. Then the hygroscopic nature of nanodiamonds should be associated with the surface functionalities of the graphitic shell and the ultramicropores on the mesopore walls.

Nanoporosity Change on Elastic Relaxation of Partially Folded Graphene Monoliths

Fabrication of nanographene shows a promising route for production of designed porous carbons, which is indispensable for highly efficient molecular separation and energy storage applications. This process requires a better understanding of the mechanical properties of nanographene in their aggregated structure. We studied the structural and mechanical properties of nanographene monoliths compressed at 43 MPa over different times from 3 to 25 h. While in monoliths compressed over shorter time adsorption isotherms of Ar at 87 K or N2 at 77 K exhibited a prominent hysteresis due to presence of predominant mesopores, compression for long time induces a low pressure hysteresis. On the other hand, compression for 25 h increases the microporosity evaluated by Ar adsorption, not by N2 adsorption, indicating that 25 h compression rearranges the nanographene stacking structure to produce ultramicropores that can be accessible only for Ar. TEM, X-ray diffraction, and Raman spectroscopic studies indicated that the compression for 25 h unfolds double-bent-like structures, relaxing the unstable nanographene stacked structure formed on the initial compression without nanographene sheets collapse. This behavior stems from the highly elastic nature of the nanographenes.